A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921455



Internal ID22696679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74114772..74115279hg38UCSC Ensembl
chr7:73529102..73529609hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38508
hg19508
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439005
Samples
Known GenesLIMK1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921455
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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